Project Manager B: Protocol Development, Clinical Statistics and Data Analyses
Tasks
- Analyze clinical outcomes databases
- Conduct study initiation visits
- Conduct study qualification visits
- Create analytic files
- Create study databases
- Develop study protocols
- Draft investigator initiated protocols
- Draft manuscripts for peer reviewed journals
- Ensure protocol compliance
- Integrate databases with statistics programs
- Issue data queries
- Manage clinical trial operations
- Monitor Adverse Events reporting
- Monitor Serious Adverse Events reporting
- Negotiate clinical trial budgets with sponsors
- Perform statistical algorithms for hypothesis testing
- Prepare NIH grant sections
- Prepare annual reports to regulatory authorities
- Prepare case report forms
- Prepare clinical trial budgets
- Prepare informed consent forms
Perks/Benefits
- Flexible work hours
- Health insurance
- Paid time off
- Professional development
- Retirement plans
- Tuition assistance
- Wellness programs
Skills/Tech-stack
Adverse Event | Case Report Form | Clinical Practice | Clinical Research | Clinical trial | Data Analysis | Data Capture | Database Design | Electronic Data | Electronic data capture | Good Clinical Practice | Grant Writing | Informed consent | Manuscript writing | NIH Grants | Protocol development | Qualitative Data | Qualitative data analysis | Quantitative data | Quantitative data analysis | SAS | Serious Adverse Event | Stata
Education
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